Nano-structured Pt-Cr anode catalyst over carbon support, for direct methanol fuel cell

被引:52
作者
Choi, Jae-Sik
Chung, Won Seob
Ha, Heung Yong
Lim, Tae-Hoon
Oh, In-Hwan
Hong, Seong-Ahn
Lee, Ho-In [1 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151744, South Korea
[2] Seoul Natl Univ, Res Ctr Energy Convers & Storage, Seoul 151744, South Korea
[3] Pusan Natl Univ, Sch Mat Sci & Engn, Pusan 609735, South Korea
[4] Korea Inst Sci & Technol, Fuel Cell Res Lab, Seoul 136791, South Korea
关键词
direct methanol fuel cell; platinum; carbon; methanol electro-oxidation;
D O I
10.1016/j.jpowsour.2005.05.075
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, several kinds of carbon were used as the support for the Pt-based catalyst of the direct methanol fuel cell (DMFC). Mesoporous carbons with large BET surface area and a commercial carbon were used as the support for the anode catalyst. The maximum current densities of the catalysts were compared by cyclic voltammogram. The catalyst supported on Vulcan XC-72, the commercial carbon support, showed the highest catalytic activity because of its high electric conductivity in spite of small BET surface area. Transition metals such as Cr, Mn, Y, or Zn were impregnated simultaneously with a Pt precursor on Vulcan XC-72, respectively, and then the catalytic activity was tested. The Pt-Cr/C catalyst showed the highest catalytic activity among this catalyst series, and was more active than the Pt/C catalyst. Furthermore, in order to improve the activity of the Pt-Cr/C catalyst, sintering of active metals by thermal reduction during the preparation should be avoided. Therefore, alkaline aluminum leaching method was applied for the purpose of decreasing the particle size of the active metals by reducing the sintering of Pt and Cr. Aluminum precursor was introduced together with Pt and Cr precursors into the commercial carbon support in the preparation process. After reduction of the sample, aluminum species were selectively leached out. The catalyst showed a much improved activity as expected and characterized by H-2 chemisorption and TEM analyses. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:466 / 471
页数:6
相关论文
共 19 条
[1]  
Aricò AS, 2001, FUEL CELLS, V1, P133
[2]  
Carrette L, 2001, FUEL CELLS, V1, P5, DOI 10.1002/1615-6854(200105)1:1<5::AID-FUCE5>3.0.CO
[3]  
2-G
[4]  
Choi Jae-Sik, 2005, [JOURAL OF KOREAN POWER METALLURGY INSTIT, 한국분말야금학회지], V12, P117
[5]  
CHUNG WS, 2003, 27 KSIEC M
[6]   Preparation of carbon-supported PtRu nanoparticles for direct methanol fuel cell applications - a comparative study [J].
Deivaraj, TC ;
Lee, JY .
JOURNAL OF POWER SOURCES, 2005, 142 (1-2) :43-49
[7]   Mechanism and electrocatalysis in the direct methanol fuel cell [J].
Hamnett, A .
CATALYSIS TODAY, 1997, 38 (04) :445-457
[8]   Scalable parallel data mining for association rules [J].
Han, EH ;
Karypis, G ;
Kumar, V .
IEEE TRANSACTIONS ON KNOWLEDGE AND DATA ENGINEERING, 2000, 12 (03) :337-352
[9]   Temperature-programmed desorption (TPD) of water from iron, chromium, nickel and 304L stainless steel [J].
Joly, JP ;
Gaillard, F ;
Peillex, E ;
Romand, M .
VACUUM, 2000, 59 (04) :854-867
[10]  
KINOSHITA K, 1988, CARBON ELECTROCHEMIC, P73